chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	263913989	263913990	A	G	52	GENIC	homozygous	108634368
1	263914210	263914211	T	C	41	GENIC	homozygous	108634370
1	263914932	263914933	C	T	42	GENIC	homozygous	108634372
1	263915547	263915547		TGT	44	GENIC	possibly homozygous	127508251
1	263917069	263917070	C	T	43	GENIC	homozygous	108634374
1	263917124	263917125	T	C	39	GENIC	homozygous	108634376
1	263917165	263917166	C	T	28	GENIC	homozygous	108634379
1	263917246	263917247	A	G	34	GENIC	homozygous	108634381
1	263917407	263917408	A	C	38	GENIC	possibly homozygous	108634383
1	263918054	263918055	A		45	GENIC	possibly homozygous	127508252
1	263918066	263918067	G	A	48	GENIC	homozygous	108634387
1	263919098	263919099	T	C	48	GENIC	homozygous	108634388
1	263919321	263919322	C	T	48	GENIC	homozygous	108634390
1	263919732	263919733	G	A	48	GENIC	homozygous	108634392
1	263919763	263919764	C	T	41	GENIC	homozygous	108634394
1	263919802	263919803	C	T	36	GENIC	homozygous	108634396
1	263919877	263919878	T	C	39	GENIC	homozygous	108634397
1	263920743	263920744	A	G	45	GENIC	homozygous	108634399
1	263920702	263920703	T		43	GENIC	homozygous	127508253